AB65978
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
10g | 98% | in stock | $14.00 | $10.00 | - + | |
25g | 98% | in stock | $28.00 | $20.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB65978 |
Chemical Name: | 4-(Dimethyl-tert-butylsilyloxy)butan-1-ol |
CAS Number: | 87184-99-4 |
Molecular Formula: | C10H24O2Si |
Molecular Weight: | 204.3818599999999 |
MDL Number: | MFCD04974070 |
SMILES: | OCCCCO[Si](C(C)(C)C)(C)C |
4-((tert-Butyldimethylsilyl)oxy)butan-1-ol, also known as $name$, is a versatile chemical compound widely used in organic synthesis as a protecting group reagent. This compound plays a crucial role in protecting alcohol functionalities during various chemical transformations, ensuring selectivity and control over chemical reactions.In chemical synthesis, $name$ is particularly valuable in the protection of primary alcohols. By forming a tert-butyldimethylsilyl (TBDMS) ether linkage with the hydroxyl group of the alcohol, $name$ effectively shields the alcohol functionality from unwanted reactions or side reactions that may occur during subsequent synthetic steps. This protection is essential in complex organic synthesis processes where multiple functional groups are present, as it allows chemists to manipulate and modify the molecule selectively.The TBDMS group introduced by $name$ is stable under a variety of reaction conditions commonly encountered in organic synthesis, such as basic or acidic conditions, making it a reliable choice for protecting alcohol groups. Furthermore, this protecting group can be removed selectively using fluoride-based reagents, providing flexibility in the deprotection strategy and enabling the recovery of the original alcohol functionality for further chemical transformations.In summary, the application of 4-((tert-Butyldimethylsilyl)oxy)butan-1-ol as a protecting group reagent in chemical synthesis enhances the efficiency and precision of organic reactions, facilitating the synthesis of complex molecules with desired functional group manipulations.